Incidental Mutation 'R4038:Vmn1r218'
ID |
313806 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Vmn1r218
|
Ensembl Gene |
ENSMUSG00000115020 |
Gene Name |
vomeronasal 1 receptor 218 |
Synonyms |
V1ri5 |
MMRRC Submission |
040965-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.140)
|
Stock # |
R4038 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
13 |
Chromosomal Location |
23320655-23321551 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 23320971 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Alanine
at position 26
(V26A)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000154769
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000074992]
[ENSMUST00000226692]
[ENSMUST00000227050]
[ENSMUST00000227160]
[ENSMUST00000227741]
|
AlphaFold |
Q8R261 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000074992
AA Change: V106A
PolyPhen 2
Score 0.906 (Sensitivity: 0.82; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000074519 Gene: ENSMUSG00000115020 AA Change: V106A
Domain | Start | End | E-Value | Type |
Pfam:TAS2R
|
1 |
288 |
2e-7 |
PFAM |
Pfam:V1R
|
33 |
297 |
5.4e-41 |
PFAM |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000226692
AA Change: V106A
PolyPhen 2
Score 0.906 (Sensitivity: 0.82; Specificity: 0.94)
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000227050
AA Change: V106A
PolyPhen 2
Score 0.906 (Sensitivity: 0.82; Specificity: 0.94)
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000227160
AA Change: V26A
PolyPhen 2
Score 0.906 (Sensitivity: 0.82; Specificity: 0.94)
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000227741
AA Change: V26A
PolyPhen 2
Score 0.226 (Sensitivity: 0.91; Specificity: 0.88)
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000228348
|
Meta Mutation Damage Score |
0.1795 |
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.7%
- 20x: 93.1%
|
Validation Efficiency |
93% (39/42) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ate1 |
A |
G |
7: 130,106,495 (GRCm39) |
S282P |
probably damaging |
Het |
Cacna1d |
T |
A |
14: 29,788,040 (GRCm39) |
Q1610L |
probably damaging |
Het |
Carmil2 |
C |
A |
8: 106,422,039 (GRCm39) |
R1103S |
probably damaging |
Het |
Clca3a1 |
T |
A |
3: 144,460,994 (GRCm39) |
Y219F |
probably benign |
Het |
Creb3l3 |
A |
G |
10: 80,925,172 (GRCm39) |
V224A |
probably benign |
Het |
Crnkl1 |
T |
A |
2: 145,774,247 (GRCm39) |
D72V |
possibly damaging |
Het |
Dhcr24 |
T |
C |
4: 106,431,075 (GRCm39) |
F255L |
probably benign |
Het |
Eef2kmt |
A |
T |
16: 5,063,135 (GRCm39) |
V335D |
probably damaging |
Het |
Elp2 |
T |
A |
18: 24,767,405 (GRCm39) |
W696R |
probably damaging |
Het |
Glb1l3 |
A |
C |
9: 26,740,343 (GRCm39) |
M329R |
probably damaging |
Het |
Gm4787 |
A |
T |
12: 81,425,132 (GRCm39) |
F342Y |
probably damaging |
Het |
Gpr137c |
C |
A |
14: 45,457,687 (GRCm39) |
L80I |
probably damaging |
Het |
Gpr83 |
A |
G |
9: 14,772,073 (GRCm39) |
I82V |
possibly damaging |
Het |
Greb1l |
C |
T |
18: 10,515,209 (GRCm39) |
T558I |
possibly damaging |
Het |
Hnrnpul2 |
T |
A |
19: 8,800,591 (GRCm39) |
|
probably benign |
Het |
Hspa2 |
T |
C |
12: 76,452,542 (GRCm39) |
V412A |
probably damaging |
Het |
Iqcd |
T |
C |
5: 120,740,587 (GRCm39) |
V306A |
probably damaging |
Het |
Lmod3 |
T |
C |
6: 97,225,275 (GRCm39) |
N182S |
probably benign |
Het |
Metrn |
T |
C |
17: 26,013,984 (GRCm39) |
T281A |
probably benign |
Het |
Mid1-ps1 |
G |
A |
Y: 90,773,563 (GRCm39) |
|
noncoding transcript |
Het |
Mmachc |
T |
A |
4: 116,563,215 (GRCm39) |
T47S |
probably damaging |
Het |
Nfia |
C |
A |
4: 97,909,074 (GRCm39) |
R277S |
probably damaging |
Het |
Or9m2 |
T |
A |
2: 87,821,262 (GRCm39) |
I269N |
possibly damaging |
Het |
Pcdha8 |
T |
C |
18: 37,125,914 (GRCm39) |
M132T |
probably benign |
Het |
Prkaa2 |
T |
C |
4: 104,908,444 (GRCm39) |
N144D |
probably damaging |
Het |
Ptprf |
C |
T |
4: 118,114,805 (GRCm39) |
R150H |
probably damaging |
Het |
Sfmbt1 |
T |
G |
14: 30,509,449 (GRCm39) |
D309E |
probably damaging |
Het |
Skint5 |
G |
T |
4: 113,743,011 (GRCm39) |
T352K |
unknown |
Het |
Slc16a10 |
G |
C |
10: 39,932,620 (GRCm39) |
H314D |
possibly damaging |
Het |
Slc28a2 |
C |
A |
2: 122,284,996 (GRCm39) |
A328E |
probably benign |
Het |
Ssc4d |
C |
A |
5: 135,999,170 (GRCm39) |
W11L |
possibly damaging |
Het |
Sycp2 |
C |
A |
2: 178,022,720 (GRCm39) |
M470I |
possibly damaging |
Het |
Tfap2c |
A |
T |
2: 172,398,110 (GRCm39) |
S413C |
probably damaging |
Het |
Unc13c |
A |
G |
9: 73,441,188 (GRCm39) |
|
probably null |
Het |
Wipf3 |
G |
A |
6: 54,458,813 (GRCm39) |
G56D |
probably damaging |
Het |
Wiz |
T |
C |
17: 32,578,198 (GRCm39) |
E429G |
probably damaging |
Het |
Zer1 |
T |
C |
2: 29,997,535 (GRCm39) |
N457S |
probably damaging |
Het |
Zfp931 |
T |
A |
2: 177,709,777 (GRCm39) |
Q203L |
possibly damaging |
Het |
|
Other mutations in Vmn1r218 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02014:Vmn1r218
|
APN |
13 |
23,321,001 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02670:Vmn1r218
|
APN |
13 |
23,321,174 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03085:Vmn1r218
|
APN |
13 |
23,321,481 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL03334:Vmn1r218
|
APN |
13 |
23,320,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R0049:Vmn1r218
|
UTSW |
13 |
23,321,225 (GRCm39) |
nonsense |
probably null |
|
R0049:Vmn1r218
|
UTSW |
13 |
23,321,225 (GRCm39) |
nonsense |
probably null |
|
R1387:Vmn1r218
|
UTSW |
13 |
23,321,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R1959:Vmn1r218
|
UTSW |
13 |
23,320,683 (GRCm39) |
missense |
probably damaging |
0.96 |
R3713:Vmn1r218
|
UTSW |
13 |
23,321,081 (GRCm39) |
missense |
probably damaging |
1.00 |
R3714:Vmn1r218
|
UTSW |
13 |
23,321,081 (GRCm39) |
missense |
probably damaging |
1.00 |
R4037:Vmn1r218
|
UTSW |
13 |
23,320,971 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4039:Vmn1r218
|
UTSW |
13 |
23,320,971 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4432:Vmn1r218
|
UTSW |
13 |
23,321,412 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5255:Vmn1r218
|
UTSW |
13 |
23,320,881 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5521:Vmn1r218
|
UTSW |
13 |
23,320,743 (GRCm39) |
missense |
probably benign |
0.01 |
R7384:Vmn1r218
|
UTSW |
13 |
23,320,895 (GRCm39) |
missense |
probably benign |
0.00 |
R7565:Vmn1r218
|
UTSW |
13 |
23,320,830 (GRCm39) |
missense |
probably benign |
0.05 |
R8178:Vmn1r218
|
UTSW |
13 |
23,321,472 (GRCm39) |
missense |
probably benign |
0.08 |
R8536:Vmn1r218
|
UTSW |
13 |
23,321,535 (GRCm39) |
missense |
probably benign |
0.00 |
R9225:Vmn1r218
|
UTSW |
13 |
23,320,824 (GRCm39) |
missense |
probably benign |
0.04 |
R9609:Vmn1r218
|
UTSW |
13 |
23,320,839 (GRCm39) |
missense |
probably benign |
0.01 |
R9734:Vmn1r218
|
UTSW |
13 |
23,321,034 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- TACACTTCTGCCTTGGGGAC -3'
(R):5'- TGAATGTTGCAGCTACAGACCTG -3'
Sequencing Primer
(F):5'- TTCTGCCTTGGGGACTGAGAAAAG -3'
(R):5'- GTTGCAGCTACAGACCTGTTCAAG -3'
|
Posted On |
2015-04-30 |